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1020-40-2

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1020-40-2 Usage

General Description

N-(2-sulfanylphenyl)benzamide is a chemical compound with the molecular formula C13H11NO2S. It is a benzamide derivative with a sulfanylphenyl group attached to the nitrogen atom. N-(2-sulfanylphenyl)benzamide is commonly used in medicinal chemistry and pharmaceutical research due to its potential biological activities. N-(2-sulfanylphenyl)benzamide has been studied for its anti-inflammatory, anticancer, and antimicrobial properties. It may also have potential applications in drug development and as a building block for the synthesis of other bioactive molecules. Additionally, N-(2-sulfanylphenyl)benzamide has shown promise in the treatment of certain diseases and conditions, making it a subject of ongoing scientific investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 1020-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1020-40:
(6*1)+(5*0)+(4*2)+(3*0)+(2*4)+(1*0)=22
22 % 10 = 2
So 1020-40-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H11NOS/c15-13(10-6-2-1-3-7-10)14-11-8-4-5-9-12(11)16/h1-9,16H,(H,14,15)

1020-40-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-sulfanylphenyl)benzamide

1.2 Other means of identification

Product number -
Other names N-benzoyl-o-aminothiophenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1020-40-2 SDS

1020-40-2Relevant articles and documents

Zeolite-catalyzed simple synthesis of different heterocyclic rings, part 2

Hegedues, Adrienn,Vigh, Ilona,Hell, Zoltan

, p. 428 - 431 (2004)

A simple and environmentally friendly synthesis was developed for the preparation of 2-arylimidazoline derivatives and 2-arylbenzoxazole derivatives using a small pore size zeolite. The similar reaction was not applicable to the preparation of the sulfur-containing analogs cysteamine or 2-aminothiophenol, probably because of a disadvantageous reaction between the zeolite and the thio compound.

Synthesis of C- and N-Substituted 1,5,2,6-Dithiadiazocanes –Electrophilic-Nucleophilic Thioamination (ENTA) Reagents

Bagd?iūnas, Gintautas,Javorskis, Tomas,Jurys, Arminas,Orentas, Edvinas

, p. 3329 - 3335 (2021/07/02)

A synthetic method is presented for S?N bond formation starting from cheap and affordable materials. We show that (un)substituted N-protected cyclic eight-membered C2-symmetric sulfenamides have been prepared in a few steps using this procedure. The synthetic utility of these ambipolar derivatives was demonstrated in a variety of synthetic transformations affording different S,N-heterocyles of pharmaceutical relevance in one or two steps from simple starting materials. (Figure presented.).

THERMAL REARRANGEMENT OF O-THIOACYL DERIVATIVES OF N-ACYL-N-ARYLHYDROXYLAMINES

Drozd, V.N.

, p. 317 - 326 (2007/10/02)

The ability of the Ar-N-O-C=S system of atoms to undergo a thermal rearrangement of the Claisen type was investigated.On the basis of the experimental data it was concluded that the process is predominantly nonconcerted in nature.

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